TRI-UNION FROZEN PRODUCTS INC DBA CHICKEN OF THE SEA FROZEN FOOD Recall: Frozen Raw Peeled & Deveined tail on, shrimp contains undeclared sulfites

🇺🇸 United States

1. May 6, 2025 - Recall initiated
2. July 2, 2025 - Reported by source
3. July 1, 2025 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-0068-2025

Event ID

97002

Status

Terminated

Classification

Class I

Company

TRI-UNION FROZEN PRODUCTS INC DBA CHICKEN OF THE SEA FROZEN FOOD

Product description

Frozen Shrimp- packaged in 5lb frozen IQF blocks/4 blocks to a case. Unlabeled generic case packaging reads: "Raw P&D Tail-On White Shrimp" 26/30; Contains: Shrimp (Crustacean) UPC# 1 08432370 0405 5

Quantity

64,000 pounds (3200 cases)

Reason

Frozen Raw Peeled & Deveined tail on, shrimp contains undeclared sulfites

Recall initiation date

May 6, 2025

Report date

July 2, 2025

Classification date

Not published in this source record

Termination date

July 1, 2025

Distribution pattern

Affected lots were sold exclusively to Whole Foods USA. Whole Foods uses some of the product for its retail in-store deli. Product was distributed to various Whole Foods stores across the country. The remaining portion of the lot, is passed through to a downstream customer in Canada (Seven Seas Fish Co. LTD).

UPC, lot, and code information

Lot# 669/18WH/124; 669/19WH/134; 669/20WH144; 669/30VH/127; 669/01HH/003; 669/03HH011 Best BY: Jul 18, 2026; Jul 19, 2026; Jul 20,2026; Sep 30,2026; Oct 01,2026; Oct 03,2026

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Other

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: TRI-UNION FROZEN PRODUCTS INC DBA CHICKEN OF THE SEA FROZEN FOOD

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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